Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1395881.RAfidkopk-NOoyCQy5bdmtBBtgJM0K7LFWieFTvk2dJFw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1395881.RAfidkopk-NOoyCQy5bdmtBBtgJM0K7LFWieFTvk2dJFw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1395881.RAfidkopk-NOoyCQy5bdmtBBtgJM0K7LFWieFTvk2dJFw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1395881.RAfidkopk-NOoyCQy5bdmtBBtgJM0K7LFWieFTvk2dJFw130_provenance.
- NP1395881.RAfidkopk-NOoyCQy5bdmtBBtgJM0K7LFWieFTvk2dJFw130_assertion description "[The clinical features of these patients were late onset progressive pure cerebellar ataxia with dysarthria and nystagmus, and are consistent with autosomal dominant cerebellar ataxia type III (ADCA type III).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1395881.RAfidkopk-NOoyCQy5bdmtBBtgJM0K7LFWieFTvk2dJFw130_provenance.
- NP1395881.RAfidkopk-NOoyCQy5bdmtBBtgJM0K7LFWieFTvk2dJFw130_assertion evidence source_evidence_literature NP1395881.RAfidkopk-NOoyCQy5bdmtBBtgJM0K7LFWieFTvk2dJFw130_provenance.
- NP1395881.RAfidkopk-NOoyCQy5bdmtBBtgJM0K7LFWieFTvk2dJFw130_assertion SIO_000772 9600677 NP1395881.RAfidkopk-NOoyCQy5bdmtBBtgJM0K7LFWieFTvk2dJFw130_provenance.
- NP1395881.RAfidkopk-NOoyCQy5bdmtBBtgJM0K7LFWieFTvk2dJFw130_assertion wasDerivedFrom befree-2016 NP1395881.RAfidkopk-NOoyCQy5bdmtBBtgJM0K7LFWieFTvk2dJFw130_provenance.
- NP1395881.RAfidkopk-NOoyCQy5bdmtBBtgJM0K7LFWieFTvk2dJFw130_assertion wasGeneratedBy ECO_0000203 NP1395881.RAfidkopk-NOoyCQy5bdmtBBtgJM0K7LFWieFTvk2dJFw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1395881.RAfidkopk-NOoyCQy5bdmtBBtgJM0K7LFWieFTvk2dJFw130_provenance.